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3-HYDROXY-7-METHOXY-2,2,10-TRIMETHYL-2,3,4,10-TETRAHYDRO-5H-PYRANO-[2,3-B]-QUINOLIN-5-ONE;O-METHYL-RIBALINIDINE

Compound with spectra: 3 NMR

3-HYDROXY-7-METHOXY-2,2,10-TRIMETHYL-2,3,4,10-TETRAHYDRO-5H-PYRANO-[2,3-B]-QUINOLIN-5-ONE;O-METHYL-RIBALINIDINE
SpectraBase Compound ID FPeffOp2lVw
InChI InChI=1S/C16H19NO4/c1-16(2)13(18)8-11-14(19)10-7-9(20-4)5-6-12(10)17(3)15(11)21-16/h5-7,13,18H,8H2,1-4H3
InChIKey ZSSWMTCWRIQOKV-UHFFFAOYSA-N
Mol Weight 289.33 g/mol
Molecular Formula C16H19NO4
Exact Mass 289.131408 g/mol

View Spectrum of 3-HYDROXY-7-METHOXY-2,2,10-TRIMETHYL-2,3,4,10-TETRAHYDRO-5H-PYRANO-[2,3-B]-QUINOLIN-5-ONE;O-METHYL-RIBALINIDINE

13C NMR Spectrum
Copyright Copyright © 2002-2025 Wiley-VCH GmbH. All Rights Reserved.
Solvent DMSO

View Spectrum of 3-HYDROXY-7-METHOXY-2,2,10-TRIMETHYL-2,3,4,10-TETRAHYDRO-5H-PYRANO-[2,3-B]-QUINOLIN-5-ONE;O-METHYL-RIBALINIDINE

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO

View Spectrum of 3-HYDROXY-7-METHOXY-2,2,10-TRIMETHYL-2,3,4,10-TETRAHYDRO-5H-PYRANO-[2,3-B]-QUINOLIN-5-ONE;O-METHYL-RIBALINIDINE

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • (+)-7-O-Methylribalinidine
5H-Pyrano[2,3-b]quinolin-5-one, 2,3,4,10-tetrahydro-3-hydroxy-7-methoxy-2,2,10-trimethyl-, (R)-
5H-Pyrano[2,3-b]quinolin-5-one, 2,3,4,10-tetrahydro-3-hydroxy-7-methoxy-2,2,10-trimethyl-, (S)-
Furo[2,3-b]quinolin-4(2H)-one, 3,9-dihydro-2-(1-hydroxy-1-methylethyl)-6-methoxy-9-methyl-, (R)-
2-(1'-HYDROXY-1'-METHYLETHYL)-6-METHOXY-9-METHYL-2,3,4,9-TETRAHYDROFURO-[2,3-B]-QUINOLIN-4-ONE;O-METHYL-RIBALINE
RIBALININE-MESYLATE
Isobalfourodine
NEOACUTIFOLIN
10H-Cyclopenta[4,5]furo[2,3-b]quinolin-10-one, 1,2,3,3a,5,10b-hexahydro-5-methyl-, cis-(.+-.)-
3,3,10-Trimethyl-2H-pyrano[2,3-b]quinolin-2,4,5(3H,10H)-trione
Lunacrine
(Z)-3-((5-chloro-2-hydroxy-4-methylphenyl)(hexylimino)methyl)-1-hexylquinolin-4(1H)-one
Title Journal or Book Year
Angular Methoxy-Substituted Furo- and Pyranoquinolinones as Blockers of the Voltage-Gated Potassium Channel Kv1.3 Journal of Medicinal Chemistry 2001
Quinoline Alkaloids From the Heartwood of Balfourodendron riedelianum Australian Journal of Chemistry 1983

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5H-Pyrano[2,3-b]quinolin-5-one, 2,3,4,10-tetrahydro-3-hydroxy-7-methoxy-2,2,10-trimethyl-, (R)-
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